CB2R PAM,98.46%
产品编号:Bellancom-131004| CAS NO:2244579-87-9| 分子式:C21H24BrFN2O2| 分子量:435.33
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CB2R PAM
产品介绍 | CB2R PAM 是一种具有口服活性大麻素 2 型受体 (CB2Rs) 正向变构调节剂。CB2R PAM 在神经病理性疼痛小鼠模型中显示抗伤害活性。 | ||||||||||||||||
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生物活性 | CB2R PAM is an orally active cannabinoid type-2 receptors (CB2Rs) positive allosteric modulator. CB2R PAM displays antinociceptive activity in vivo in an experimental mouse model of neuropathic pain. | ||||||||||||||||
体外研究 |
CB2R PAM (100 nM) significantly enhances the ability of CP55940 and 2-AG, but not of AEA, to stimulate [35S]GTPγS binding to CB2Rs. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 |
CB2R PAM (1-20 mg/kg; p.o.) displays antinociceptive activity. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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体内研究 |
CB2R PAM (1-20 mg/kg; p.o.) displays antinociceptive activity. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 50 mg/mL (114.86 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
*以上所有助溶剂都可在 西域 网站选购。
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运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) | ||||||||||||||||
参考文献 |